QUANTITATIVE METHODS TO MAP GENES FOR COMPLEX TRAITS

绘制复杂性状基因图谱的定量方法

• 批准号: 6053050
• 负责人: JURG OTT
• 金额: $ 13.78万
• 依托单位: ROCKEFELLER UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-03-01 至 2003-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6053050
• 关键词: analytical method; computer program /software; gene expression; genetic disorder; genetic markers; genetic susceptibility; genotype; linkage disequilibriums; linkage mapping; method development; quantitative trait loci; statistics /biometry

The long-term goal is to develop novel analytical methods that will enable researchers to find sets of disease genes underlying complex traits. These methods make use of genetic linkage and linkage disequilibrium between markers and nearby disease genes and provide, for example, maximum likelihood estimates for the numbers and positions of disease genes. Results are expected to open the way to identifying susceptibility genes. Once such genes are found, there is hope that knowledge of their structure will lead to a deeper understanding of disease etiology and, thus, to the possibility of ameliorating or curing these traits. The three specific aims are 1) to apply the Ising model of statistical physics to linkage and disequilibrium analysis, 2) to investigate effects of pedigree errors on disequilibrium analysis, and 3) to implement methodology developed under this proposal in computer programs.

长期目标是开发新的分析方法，使研究人员能够找到复杂性状背后的疾病基因组。这些方法利用标记和邻近疾病基因之间的遗传连锁和连锁不平衡，并提供例如疾病基因的数量和位置的最大似然估计。这些结果有望为鉴定易感基因开辟道路。一旦发现这些基因，就有希望了解它们的结构，从而更深入地了解疾病的病因，从而有可能改善或治愈这些特征。三个具体目标是：1）将统计物理学的伊辛模型应用于连锁和不平衡分析，2）调查谱系错误对不平衡分析的影响，以及3）在计算机程序中实施根据该提议开发的方法。